1887

Abstract

SUMMARY

RNA 1* (see end of Summary) of a cold-adapted and temperature-sensitive () influenza virus mutant A/Ann Arbor/6/60 has a different mobility from RNA 1 of wild-type (wt) A/Ann Arbor/6/60 when subjected to electrophoresis through acrylamide/agarose gels in the absence of denaturing agents. Detection of this lesion in RNA 1 of the mutant virus was dependent on the temperature of the gel during electrophoresis. Because RNA 1 is believed to code for a protein involved in virus-specific RNA synthesis we compared phenotypes of virion transcriptases in the wt and mutant viruses. The enzyme of the mutant virus was found to be about 40% less active at 40 °C than the enzyme of the wt virus when related to their activities at 31 °C. Two cold-adapted recombinants which derive their RNA 1 from the mutant A/Ann Arbor/6/60 have virion transcriptases with a phenotype similar to that of their mutant parent. Three different cold-adapted recombinants, however, which also derive their RNA 1 from the mutant A/Ann Arbor/6/60, have virion transcriptases with a phenotype similar to that of wt virus. We conclude, therefore, that the conditional-lethal property of A/Ann Arbor/6/60 mutant and its recombinants is independent of the phenotypic marker observed for the A/Ann Arbor/6/60 mutant virion transcriptase, and that the lesion in RNA 1 of the mutant may also be unrelated to the observed difference between virion transcriptases of the mutant and wt A/Ann Arbor/6/60 viruses. The phenotypes of the virion transcriptases in recombinants did, however, correlate with the derivation of their RNA 2. This suggests that the increased temperature-sensitivity of virion transcriptase of the A/Ann Arbor/6/60 mutant is caused by either (1) a lesion (not necessarily conditionally lethal) that occurred in its RNA 2 during the course of cold-adaptation, or (2) a lesion in another gene whose product is a component of the virion transcriptase complex, but which lesion is only expressed phenotypically when there is a synergistic interaction in the transcriptase complex with the product of A/Ann Arbor/6/60 RNA 2.

* Our nomenclature for RNAs 1, 2 and 3 relates to results of electrophoresis under reference conditions where urea is omitted from gels and water at a temperature of 38 to 39 °C is circulated through the heat exchanger of the electrophoresis apparatus. Application of this nomenclature to describe in the text results obtained with other conditions of electrophoresis has only been done where control experiments have been performed which verify the validity of such an extrapolation.

Loading

Article metrics loading...

/content/journal/jgv/10.1099/0022-1317-44-2-443
1979-08-01
2024-04-25
Loading full text...

Full text loading...

/deliver/fulltext/jgv/44/2/JV0440020443.html?itemId=/content/journal/jgv/10.1099/0022-1317-44-2-443&mimeType=html&fmt=ahah

References

  1. Bonner W. M., Laskey R. A. 1974; A film detection method for tritium-labeled proteins and nucleic acids in polyacrylamide gels. European Journal of Biochemistry 46:83–88
    [Google Scholar]
  2. Cox N. L., Kendal A. P. 1978; Effect of temperature on the order of electrophoretic migration of influenza virus neuraminidase and nucleoprotein genes in acrylamide gels lacking denaturing agents. Journal of General Virology 40:229–232
    [Google Scholar]
  3. Cox N. J., O’Neill M. C., Kendal A. P. 1977; Replication of animal viruses in differentiating muscle cells: influenza virus A. Journal of General Virology 37:161–173
    [Google Scholar]
  4. Floyd R. W., Stone M. P., Joklik W. K. 1974; Separation of single stranded ribonucleic acids by acrylamide-agarose-urea gel electrophoresis. Analytical Biochemistry 59:599–609
    [Google Scholar]
  5. Ito Y., Joklik W. K. 1972; Temperature-sensitive mutants of reovirus. H. Anomolous electrophoretic migration of certain hybrid RNA molecules composed of mutant plus strands and wild-type virus strand. Virology 50:202–208
    [Google Scholar]
  6. Kendal A. P., Kiley M. P., Maassab H. F. 1973; Comparative studies of wild-type and ‘cold mutant’ (temperature-sensitive) influenza viruses: Polypeptide synthesis by an Asian (H2N2) strain and its cold-adapted variant. Journal of Virology 12:1503–1511
    [Google Scholar]
  7. Kendal A. P., Cox N. J., Murphy B. R., Spring S. B., Maassab H. F. 1977; Comparative studies of wildtype and ‘cold-mutant’ (temperature-sensitive) influenza viruses. Genealogy of the matrix (M) and non-structural (NS) proteins in recombinant cold-adapted H3N2 viruses. Journal of General Virology 37:I45–I59
    [Google Scholar]
  8. Kendal A. P., Cox N. J., Spring S. B., & Maassab H. F. 1978; Biochemical characteristics of recombinant viruses derived at suboptimal temperatures. In Negative Strand Viruses and the Host Cell pp 733–744 Edited by Mahy B. W. J., Barry R. D. New York: Academic Press;
    [Google Scholar]
  9. Krug R. M., Ueda M., Palese P. 1975; Temperature-sensitive mutants of influenza WSN virus defective in virus-specific RNA synthesis. Journal of Virology 16:790–796
    [Google Scholar]
  10. Mcgeoch D., Kitron N. 1975; Influenza virion RNA-dependent RNA polymerase: stimulation by guanosine and related compounds. Journal of Virology 15:686–695
    [Google Scholar]
  11. McKenzie J. S. 1969; Virulence of temperature-sensitive mutants of influenza virus. British Medical Journal 3:757–758
    [Google Scholar]
  12. Maassab H. F. 1967; Adaptation and growth characteristics of influenza virus at 25 °C. Nature, London 213:612–614
    [Google Scholar]
  13. Maassab H. F., Kendal A. P., Davenport F. M. 1972; Hybrid Formation of influenza virus at 250. Proceedings of the Society for Experimental Biology and Medicine 139:768–773
    [Google Scholar]
  14. Maassab H. F., Cox N. J., Murphy B. R., Kendal A. P. 1977; Biological, genetic and biochemical characterization of a cold-adapted recombinant A/Victoria/3/75 virus and its evaluation in volunteers. In International Symposium on Influenza Immunization (II) 3925–31 Geneva, Development of biological standardization Basel: S. Karger;
    [Google Scholar]
  15. Mowshowitz S. L., Ueda M. 1976; Temperature-sensitive virion transcriptase activity in mutants of WSN influenza virus. Archives of Virology 52:135–141
    [Google Scholar]
  16. Murphy B. R., Spring S. B., Chanock R. M. 1976; Live vaccine: Production and use in influenza. In Virus, Vaccines, and Strategy pp 179–197 Edited by Selby P. New York: Academic Press;
    [Google Scholar]
  17. Paffenholz V., Scholtissek C. 1973; Mode of replication and temperature characteristics of the RNA polymerase of an influenza virus in vitro. Zeitschrift für Naturforschung 28:208–213
    [Google Scholar]
  18. Palese P., Ritchey M. B. 1977; Live attenuated influenza virus vaccines. Strains with temperaturesensitive defects in P3 protein and nucleoprotein. Virology 78:183–191
    [Google Scholar]
  19. Palese P., Ritchey M. B., Schulman J. L. 1977; P1 and P3 proteins of influenza virus are required for complementary RNA synthesis. Journal of Virology 21:1187–1195
    [Google Scholar]
  20. Plotch S. J., Krug R. M. 1977; Influenza virion transcriptase: Synthesis in vitro of large, polyadenylic acid-containing complementary RNA. Journal of Virology 21:24–34
    [Google Scholar]
  21. Spring S. B., Maassab H. F., Kendal A. P., Murphy B. R., Chanock R. M. 1977a; Cold-adapted variants of influenza virus A. I. Comparison of the genetic properties of ts mutants and 5 cold-adapted variants of influenza. Virology 77:337–343
    [Google Scholar]
  22. Spring S. B., Maassab H. F., Kendal A. P., Murphy B. R., Chanock R. M. 1977b; Cold-adapted variants of influenza A. II. Comparison of the genetic and biological properties of ts mutants and recombinants of the cold-adapted A/AA/6/60 strain. Archives of Virology 55:233–246
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jgv/10.1099/0022-1317-44-2-443
Loading
/content/journal/jgv/10.1099/0022-1317-44-2-443
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error